MECHANISM OF SUBSTITUTION AT A SATURATED CARBON ATOM .27. THE ROLE OF STERIC HINDRANCE - (SECTION-B) A COMPARISON OF THE RATES OF REACTION OF ETHYL AND NEOPENTYL BROMIDES WITH INORGANIC IODIDES IN ACETONE SOLUTION

被引：15

作者：

DOSTROVSKY, I

HUGHES, ED

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY | 1946年 / MAR期

关键词：

D O I：

10.1039/jr9460000161

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：161 / 164

页数：4

共 11 条

[1] An acetylenic analog of neopentyl bromide, evidence that the hindrance to displacement reactions in neopentyl halides is steric in nature
Bartlett, PD
Rosen, LJ
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1942, 64 : 543 - 546
[2] The relation between the structure of organic halides and the speeds of their reaction with inorganic iodides. II. A study of the alkyl chlorides
Conant, JB
Hussey, RE
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1925, 47 : 476 - 488
[3] CONANT JB, 1924, J AM CHEM SOC, V46, P245
[4] HAMMETT, 1940, PHYSICAL ORGANIC CHE, P154
[5] HUGHES, 1935, J CHEM SOC, P1525
[6] HUGHES, 1935, J CHEM SOC, P244
[7] LANG, 1922, Z ANORG CHEM, V122, P332
[8] LANG, 1925, Z ANORG CHEM, V144, P75
[9] LANG, 1925, Z ANORG ALLG CHEM, V142, P279
[10] A new jodometric method, which is based on the formation and measurement of iodine cyanide II.
Lang, R
[J]. ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1925, 142 (3/4): : 229 - 256